A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17848423



Internal ID22032066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:35478351..35478351hg38UCSC Ensembl
chr1:35943952..35943952hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6242242
Supporting Variants
Samples
Known GenesKIAA0319L
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17848423
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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